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ChemicalBook--->CAS DataBase List--->474-58-8

474-58-8

474-58-8 Structure

474-58-8 Structure
IdentificationBack Directory
[Name]

ELEUTHEROSIDE A
[CAS]

474-58-8
[Synonyms]

BSSG
lyoniside
ALEXANDRIN
doursterol
aucosterol
DAUCOSTEROL
daucosterin
SITOGLUSIDE
coriandrinol
ELEUTHEROSIDE A
Carrot glycoside
sitosterylglycoside
sitosterold-glucoside
beta-sitosterylglucoside
beta-sitosterolglucoside
ELEUTHEROSIDE A USP/EP/BP
ELEUTHEROSIDE A 474-58-8
B-SITOSTEROL-3-O-GLUCOSIDE
Β-SITOSTEROL Β-D-GLUCOSIDE
beta-sitosterolmonoglucoside
BETA-SITOSTEROL-3-O-GLUCOSIDE
Β-SITOSTEROL-D-GLUCOSIDE 10%
Eleutheroside A (=Daucosterol)
SITOSTEROL-3-O-GLUCOSIDE, BETA-
B-SITOSTEROL B-D-GLUCOPYRANSIDE
β-Sitosterol 3-O-β-D-glucopyranoside
β-sitosterol-3-O-β-D-glucopyranoside
STIGMAST-5-EN-3-O-B-D-GLUCOPYRANOSIDE
Stigmast-5-en-3β-yl β-D-glucopyranoside
(3β)-Stigmast-5-en-3-yl β-D-glucopyranoside
β-D-Glucopyranoside, (3β)-stigMast-5-en-3-yl
3-beta-(beta-d-glucopyranosyloxy)-stigmast-5-en
3-beta-(beta-d-glucopyranosyloxy)stigmast-5-ene
(17xi)-stigmast-5-en-3-yl beta-D-glucopyranoside
(3-beta)-stigmast-5-en-3-yl-beta-d-glucopyranosid
(3-beta)-stigmast-5-en-3-yl-beta-d-glucopyranoside
sodium 4,6-dioxo-1,4,5,6-tetrahydropyrimidin-2-olate
DaucosterolQ: What is Daucosterol Q: What is the CAS Number of Daucosterol Q: What is the storage condition of Daucosterol
(2R,3R,4S,5R,6R)-2-[[(8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methyl-heptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
[EINECS(EC#)]

1592732-453-0
[Molecular Formula]

C35H60O6
[MDL Number]

MFCD01683621
[MOL File]

474-58-8.mol
[Molecular Weight]

576.85
Chemical PropertiesBack Directory
[Melting point ]

283~286℃
[Boiling point ]

673.6±55.0 °C(Predicted)
[density ]

1.13±0.1 g/cm3(Predicted)
[Fp ]

361℃
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO (Slightly,Heated), Pyridine (Slightly, Sonicated)
[form ]

neat
[pka]

12.91±0.70(Predicted)
[color ]

Off-White to Pale Beige
[InChIKey]

YITHQYDRZAVJHB-WWJUBMRMSA-N
[LogP]

8.615 (est)
Safety DataBack Directory
[Safety Statements ]

24/25
[WGK Germany ]

3
[HS Code ]

29389090
[Toxicity]

LD50 intraperitoneal in mouse: 62mg/kg
Questions And AnswerBack Directory
[Uses]

Daucosterol can be used as an efficient and inexpensive neuroprotectants, to which the IGF1-like activity of daucosterol contributes and it could be potentially developed as a medicine for ischemic stroke treatment. Moreover, daucosterol has neuroprotective activity, it has proliferation-enhancing activity of neural stem cells (NSCs), and it as an efficient and inexpensive growth factor alternative that could be potentially developed as a medicine for ischemic stroke treatment, can significantly reduce neuronal loss.
The study demonstrated that daucosterol works as an efficient and inexpensive growth factor alternative that could be used in clinical medicine and research applications.

[Description]

Daucosterol, alias: Citoside, β-Sitosterol β-D-glucoside, and the molecular formula is C35H6. The compound of the formula (description column) belongs to a carotene compound, which is present in mallow family plants, and figs and other plants also contain carotene. Daucosterol exhibits anti-tumor, anti-inflammatory and acaricidal activities, also moderate antibacterial activity against Bacillus subtilis and Staphylococcus aureus, and it has anti-cancer and apoptotic effects in human colon cancer cell line HCT-116.

Hazard InformationBack Directory
[Chemical Properties]

White to off white powder
[Definition]

ChEBI: A steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruti osa.
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